Computer-based methods of designing molecules

ABSTRACT

The invention features a method of generating an immunogenic compound with the ability to induce an immune response to a molecule produced by a pathogenic agent, e.g., a infectious agent or a tumor cell. Also included in the invention are an immunogenic compound generated by the method of the invention and a method of inducing an immune response in a mammal that involves administering the immunogenic compound to the mammal.

The work described in this application was supported in part by grant numbers AI43649 and AI50900 from the National Institute for Allergy and Immunological Diseases (NIAID). Thus the Government may have certain rights in the invention.

TECHNICAL FIELD

This invention relates to computer-based methods of designing molecules.

BACKGROUND

In view of the human and economic devastation inflicted by infectious diseases such as AIDS and malaria and malignant diseases such as breast and prostate cancer, it is imperative that immunogens be developed that can be used as prophylactic and/or therapeutic agents against them.

SUMMARY

The inventors have discovered a computer-based method for designing a compound useful for eliciting antibodies specific for a particular pathogenic agent. The method involves identifying the three-dimensional (3-D) structure of a segment of a pathogenic agent-derived, biological molecule (e.g., a protein) (designated herein as a pathogenic factor) that is likely to be an effective pathogenic agent-specific immunogen. Having obtained the 3-D structure of such a segment, a compound (e.g., a peptide) with essentially the same 3-D structure as the segment is synthesized and tested for its ability to elicit the production of antibodies in a mammalian host; such antibodies will preferably (though not necessarily) be protective from the pathogenic effect of a relevant pathogenic agent. A compound with the capacity to elicit the production of antibodies can then be manufactured.

More specifically, the invention features a computer-assisted method of generating an immunogen. The method requires the use of a programmed computer that includes a processor and an input device. The method involves: (a) providing a pathogenesis factor (PF), or a fragment of a PF, that contains a region with low polymorphism, the region being in an active conformation and being on an external surface of the PF; (b) obtaining data on the region in the active conformation, the data being useful for the determination of the three-dimensional structure of the region in the active conformation; (c) inputting to the input device the data; (d) determining, using the processor, the three-dimensional structure of the region in the active conformation; (e) designing a compound containing a domain that includes at least one epitope with the ability to induce the production in a mammal of an antibody that binds to the region in the active conformation; (f) producing the compound; and (g) determining whether the compound is an immunogen in a mammalian host. The PF can be a component, or an altered form of a component, of an infectious microorganism. In addition, the antibody that binds to the region in the active conformation can be an antibody that binds to a plurality of (e.g., two, three, four, five, six, seven, eight, nine, ten, 15, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 300, 500, 750, 1000, 1,500, 2000, 3,000, 5,000, 10,000, 20,000, 30,000, or all) strains (or isolates) of the infectious microorganism. The infectious microorganism can be a microorganism that replicates inside a cell. It can be a virus, e.g., a retrovirus such as simian immunodeficiency virus (SIV) or human immunodeficiency virus (HIV). The microorganism can also be a protozoan parasite, e.g., malarial protozoan parasite, and the PF can be, for example, merozoite surface protein-1 (MSP-1), ring-infected erythrocyte surface antigen (RESA), Plasmodium falciparum erythrocyte membrane protein-1(PfiMP-1), Plasmodium falciparum 332 antigen (pf332), Rosettin, merozoite surface protein-2 (MSP-2), serine stretch protein (SERP), glutamate-rich protein (GLURP), apical membrane antigen-i (AMA-1), or histidine-rich protein-2 (HRP-2). Alternatively the microorganism can be a bacterium such as any of those listed herein. The PF, or a wild-type form of the PF, can mediate entry of the microorganism into a cell. Such a cell can be a CD4+ cell such as a T cell or a monocyte or a macrophage. The cell can also be, for example, an erythrocyte. The PF can be: (a) a naturally occurring polypeptide; (b) an altered form of a naturally occurring polypeptide; or (c) a molecular complex comprising two or more subunits, each subunit being either of (a) or (b). The PF can include a complex of retroviral envelope glycoproteins or recombinant forms of such proteins, e.g., it can contain three recombinant SIV gp140 polypeptides. The PF can also be a component, or an altered form of a component, of a cancer cell, e.g., prostate-specific membrane antigen (PSMA) or any other tumor cell surface molecule. The PF can be provided in a crystalline form and the data can be a criteria data set that includes three-dimensional atomic coordinates.

The invention also includes a process of manufacturing a compound. The process involves: carrying out the above-described computer-assisted method of generating an immunogen; and, after determining that the compound is an immunogen, manufacturing the compound.

Another aspect of the invention is a method of testing a compound for prophylactic activity. The method involves administering a compound manufactured by the above-described method of manufacturing a compound to a mammal and testing for the presence in the mammal of antibodies that inhibit the pathogenicity of a pathogenic agent of which the PF is (a) a component or (b) an altered form of a component. In this method, the presence in the mammal of antibodies that inhibit the pathogenicity of the pathogenic agent is an indication that the compound has prophylactic activity against the pathogenic agent.

Another aspect of the invention is a compound manufactured by the above-described process of manufacturing a compound. The invention provides a method of inducing an immune response in a mammal. The method involves administering the above-described compound of the invention to the mammal. The compound can be administered to the mammal parenterally, intranasally, transcutaneously, or by any other route recited herein. The immune response can be a protective immune response and, as such, is preferably protective against a plurality of (e.g., two, three, four, five, six, seven, eight, nine, ten, 15, 20, 30, 40, 50, 60, 70, 80, 90, 100, 150, 200, 300, 500, 750, 1000, 1,500, 2000, 3,000, 5,000, 10,000, 20,000, 30,000, or all) strains (or isolates) of the infectious microorganism.

As used herein, “immunogenic” means capable of eliciting a functional immune response in a B precursor cell. As used herein, a B precursor cell is a B lymphocyte that, subsequent to activation, can produce antibody molecules. Activation of a B precursor cell can be, without limitation, by recognition of an antigen by an antigen specific immunoglobulin receptor on the B precursor cell. Thus, a B precursor cell can be a “virgin” B lymphocyte that has never previously been activated or a “memory” B lymphocyte that has previously been activated or the progeny of such a B lymphocyte.

As used herein, “antigenic” means capable of being recognized by an effector B lymphocyte or an antibody molecule. Thus, a substance is antigenic if it is recognized by an antigen specific receptor on, for example, a B lymphocyte producing antibody molecules or by an antibody molecule physically unassociated with a B lymphocyte.

“Polypeptide” and “protein” are used interchangeably and mean any peptide-linked chain of amino acids, regardless of length or post-translational modification.

As used herein, an expression control sequence that is “operably linked” to a coding sequence is incorporated into a genetic construct so it effectively controls expression of the coding sequence.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. In case of conflict, the present document, including definitions, will control. Preferred methods and materials are described below, although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention. All publications, patent applications, patents and other references mentioned herein are incorporated by reference in their entirety. The materials, methods, and examples disclosed herein are illustrative only and not intended to be limiting.

Other features and advantages of the invention, e.g., designing efficacious immunogens, will be apparent from the following description, from the drawings and from the claims.

DESCRIPTION OF DRAWINGS

FIGS. 1A and 1B are bar charts showing the amino acid sequence variability of each amino acid of the gp41 ectodomain from HIV-1. Sequence variability (“VAR”) at each amino acid sequence position is represented by the Shannon entropy (H) and gp41 ectodomain positions are indicated under the bar charts with the consensus amino acid residue at that position. H values and consensus amino acid residues were derived from multiple sequence alignments of gp41 isolates from HIV-1 clades A (“A”), B (“B”), C (“C”), O (“O”), and all isolates (“ALL”), regardless of lade. The consensus amino acid residues were obtained at a 50% threshold (i.e., the indicated residue or residue type was present in at least 50% of the sequences analyzed). Upper case letters represent the relevant consensus amino acid residues. Lower case letters represent the following amino acid types: “o”, amino acids with alcohol side chains (i.e., S or T); “.” (dot), any amino acid; “c”, amino acids with charged side chains (i.e., D, E, H, K, or R); “−”, amino acids with negatively charged side chains (i.e., D or E); “p”, amino acids with polar side chains (i.e., C, D, E, H, K, N, Q, R, S, or T); “+”, amino acids with positively charged side chains (i.e., H, K, or R); “s”, amino acids with small side chains (i.e., A, C, D, G, N, P, S, T, or V); and “u”, amino acids with very small side chains (A, G, or S). Additional features shown are as follows: residues indicated by filled black boxes are cysteines that are believed to be engaged in a disulfide bridge; asparagine (N) residues framed by an open box are potential N-glycosylation sites; the boxed LDKWAS sequence (SEQ ID NO:5) is the target epitope of the 2F5 monoclonal antibody [Muster et al. (1993) J. Virol. 67(11);6642-6647]; gray shaded residues in the N-domain form the lining of a hydrophobic cavity.(observed in the x-ray crystallographically derived structure of the gp41 trimeric core [Chan et al. (1997) Cell 89(2)263-273]) which is occupied by residues of the C-domain (also shaded in gray). Underlined sequences in the loop and C domains of the ALL bar chart are sequences that are potential targets for immunogen development by the method of the invention. The various regions of gp41 (fusion peptide, N-domain, loop and C-domain) are indicated under the ALL bar chart. Additional 3-D structural information is provided under the ALL bar chart. Thus, helical regions observed in the previously described x-ray crystallographically derived structures of the trimeric gp41 core [Weissenhorn et al. (1997) Nature 387(6632):426-430; Chan et al. (1997) supra] are indicated by a filled cylinder. Secondary structure predictions, and a model of the full length gp41 [Caffrey (2001) Biochim Biophys. Acta 1536:116-122], indicate that the span of the helical regions is longer; this longer span of the helical regions is shown by an extended empty cylinder. The “a” to “g” letters under the consensus amino acids of the “ALL” bar chart mark the residues constituting the heptad repeats of the N- and C-domain helices. Interestingly, “a” and “d” residues of a given N-domain heptad repeat interact with “a” and “d” residues, respectively, of a neighboring N-domain heptad in the trimeric gp41 core structure, and residues “e” and “g” of a given C-domain heptad interact with “a” and “d” residues, respectively, of a neighboring C-domain hepad in the trimeric gp41 core structure [Chan et al. (1997) supra].

FIG. 2A: is a depiction of the nucleotide sequence (SEQ ID NO:1) of cDNA encoding simian immunodeficiency virus (SIV) strain Mac23HpJ5 gp160. The 3′ end of the leader sequence is indicated by a vertical line.

FIG. 2B is a depiction of the amino acid sequence (SEQ ID NO:2) of SIV Mac23HpJ5 gp160. The cleavage site of the N-terminal signal sequence is indicated by a vertical line.

FIG. 3A is a depiction of the nucleotide sequence (SEQ ID NO:3) of cDNA encoding recombinant SIV Mac23HpJ5 gp140. The 3′ end ofthe heterologous tissue plasminogen activator (tpA) leader sequence is indicated by a vertical line.

FIG. 3B is a depiction of the amino acid sequence (SEQ ID NO:4) of recombinant SIV Mac23HpJ5 gp140. The cleavage site of the heterologous tpA N-terminal signal sequence is indicated by a vertical line.

FIG. 4A is a depiction of the amino acid sequence (SEQ ID NO:15) of the GCG2 fusion protein.

FIG. 4B is a depiction of the amino acid sequence (SEQ ID NO:16) of the HIV-1 gp41 C-terminal ectodomain segment included in the GCG2 fusion protein.

FIG. 4C is a depiction of the amino acid sequence (SEQ ID NO:17) included in SEQ ID NO:16 that corresponds to a C-domain sequence in HIV-1 gp41 (having in the consensus sequence shown in the “ALL” chart in FIG. 1 the amino acid sequence SEQ ID NO:14) that, on account of its low polymorphism and predicted location on the surface of gp41 in its trimeric, prefusion state, is considered a promising candidate for immunogen development.

FIG. 5 is a photograph of a Coomassie blue-stained sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) gel of proteins immunoprecipitated by GammaBind Plus™ beads (Amersham Biosciences, Piscataway, N.J.) coated with the 2F5 monoclonal antibody (mAb) (“2F5 beads”) or the 4E10 mAb (“4E10 beads”), both specific for HIV-1 gp41, that had been incubated with (“+”) or without (“−”) purified GCG2 fusion protein for 4 hours at 4° C. The right lane of the gel (“+”) contained purified GCG2 protein. The positions of molecular weight markers are shown by the numbers to the right of the photograph; the numbers are the molecular weights (kDa×10³¹ ³) of the markers.

FIG. 6 is a line graph showing the Biosensor responses (over time) observed with a CM5 chip coated with either mAb 98.6 (“98.6”) or mAb 126.6 (“126.6”) and then exposed to a solution of GCG2 fusion protein.

DETAILED DESCRIPTION

Various aspects of the invention are described below.

Computer Hardware and Software

The invention can be implemented in computer hardware or software, or a combination of both. However, the invention is preferably implemented in one or more computer programs executing on one or more programmable computers, each containing a processor and at least one input device. The computers will preferably also contain a data storage system (including volatile and non-volatile memory and/or storage elements) and at least one output device. Program code is applied to input data to perform the functions described above and generate output information. The output information is applied to one or more output devices in a known fashion. The computer can be, for example, a personal computer, microcomputer, or work station of conventional design.

Each program is preferably implemented in a high level procedural or object oriented programming language to communicate with a computer system. However, the programs can be implemented in assembly or machine language, if desired. In any case, the language can be a compiled or interpreted language.

Each computer program is preferably stored on a storage media or device (e.g., ROM or magnetic diskette) readable by a general or special purpose programmable computer. The computer program serves to configure and operate the computer to perform the procedures described herein when the program is read by the computer. The method of the invention can also be implemented by means of a computer-readable storage medium, configured with a computer program, where the storage medium so configured causes a computer to operate in a specific and predefined manner to perform the functions described herein.

For example, the computer-requiring steps in a method of designing an immunogenic compound can minimally involve:

-   -   (a) inputting into an input device, e.g., through a keyboard, a         diskette, or a tape, data that can be used to determine the 3-D         structure of a PF region having low polymorphism, e.g., a         criteria data set containing 3-D atomic co-ordinates of the         region; and     -   (b) determining, using a processor, the 3-D structure of the         region.

The method can involve the additional step of outputting to an output device a model of the 3-D structure of the region. In addition, the data can be compared to a computer database of, for example, 3-D structures stored in a data storage system.

Pathogenic Factors (PF) and Pathogenic Agents

The method of the invention involves, in part, the analysis of a pathogenesis factor region with low polymorphism.

As used herein, a “pathogenesis factor” (“PF”) is a molecule or a molecular complex that is a component of a pathogenic agent, or an altered form of such a component. Thus, PF can be wild-type molecules or complexes containing wild-type molecules. They can also be molecules, or complexes of molecules, altered from the wild-type form by, for example, chemical or recombinant methodologies, but in a way that does not change the tertiary structure of the region referred to herein as the region with low polymorphism. Thus, in a PF that is such an altered molecule or is a complex containing such an altered molecule, the region with low polymorphism will have the same tertiary structure that it has in the native conformation of the wild-type molecule. PF can be physically associated with the pathogenic agent (e.g., as a cell membrane, cell wall, or viral coat component) or it can be released or secreted from the pathogenic agent.

As used herein, a “pathogenic agent” is a biological entity that causes pathological symptoms when present in a mammalian host. Thus a pathogenic agent can be, without limitation, an infectious agent (e.g., a virus, a prion, a bacterium, a yeast or other fungus, a mycoplasma, or a eukaryotic parasite such as a protozoan parasite, a nematode parasite, or a trematode parasite) or a tumor cell (e.g., a lung cancer or a breast cancer cell). Examples of relevant infectious agents include, without limitation, Mycobacteria tuberculosis, Salmonella enteriditis, Listeria monocytogenes, M leprae, Staphylococcus aureus, Escherichia coli, Streptococcus pneumoniae, Borrelia burgdorferi, Actillobacillls pleuropneumoniae, Helicobacter pylori, Neisseria meningitidis, Yersinia enterocolitica, Bordetella pertussis, Porphyromonas gingivalis, mycoplasma, Histoplasma capsulatum, Cryptococcus neoformans, Chlamydia trachomatis, Candida albicans, Plasmodium falciparum, Plasmodium vivax, Plasmodium malariae, Entamoeba histolytica, Toxoplasma brucei, Toxoplasma gondii, Leishmania major, human immunodeficiency virus 1 and 2, influenza virus, measles virus, rabies virus, hepatitis virus A, B, and C, rotaviruses, papilloma virus, respiratory syncytial virus, feline immunodeficiency virus, feline leukemia virus, and simian immunodeficiency virus.

Examples of tumor cells include cells from neural tissue cancer, melanoma, breast cancer, lung cancer, gastrointestinal cancer, ovarian cancer, testicular cancer, lung cancer, prostate cancer, cervical cancer, bladder cancer, vaginal cancer, liver cancer, renal cancer, bone cancer, a hematological cell cancer, and vascular tissue cancer.

PF can be composed of protein, nucleic acid (DNA or RNA), carbohydrate, lipid, or a combination of two or more of these. They will preferably have at least a component that is a polypeptide. Examples of relevant infectious agent proteins include, without limitation, the B subunit of heat labile enterotoxin of E. coli [Konieczny et al. (2000) FEMS Immunol. Med. Microbiol. 27(4):321-332]; heat-shock proteins, e.g., the Y enterocolitica heat shock protein 60 [Konieczny et al. (2000) supra; Mertz et al. (2000) J. Immunol. 164(3):1529-1537] and M. tuberculosis heat-shock proteins hsp60and hsp70; the Chlamydia trachomatis outer membrane protein [Ortiz et al. (2000) Infect. Immun. 68(3): 1719-1723); the B. burgdorferi outer surface protein [Chen et al. (1999) Arthritis Rheum. 42(9):1813-1823]; the L major GP63 [White et al. (1999) Vaccine 17(17):2150-2161 (and published erratum in Vaccine 17(20-21):2755)]; the N. meningitidis meningococcal serotype 15 PorB protein [Delvig et al. (1997) Clin. Immunol. Immunopathol. 85(2);134-142]; the P. gingivalis 381 fimbrial protein [Ogawa, (1 994) J. Med. Microbiol. 41 (5):349-358]; the E. coli outer membrane protein F [Williams et al. (2000) Infect. Immun. 68(5):2535-2545]; influenza virus hemagglutinins and neuraminidases; retroviral (e.g., HIV) surface glycoproteins (e.g., I-V gp160/120), or retroviral tat or gag proteins. Examples of relevant molecules produced by tumor cells include: (a) tumor antigens such as prostate-specific membrane antigen (PSMA) [Israeli et al. (1993) Cancer Res. 53(2):227-230], a mucin such as MUC-1, or any other antigen expressed on the surface of tumor cells; and (b) tumor-produced angiogenic factors such as vascular endothelial growth factor (VEGF), VEGF-A, VEGF-B, VEGF-C, and VEGF-D [Detmar (2000) J. Investig. Dermatol. Symp. Proc. 5(1):20-23; Paweletz et al. (1989) Crit. Oncol. Hematol. 9(3):197-242].

In view of their role in binding of HIV or SIV to target cells, the CD4 binding site and the chemokine receptor binding site on gp120 would both, at first glance, seem to be good candidates regions for the development of vaccines to HIV and SIV However, there are two factors limiting the usefulness of these as candidates for vaccine development: (a) extensive inter- and intra-clade polymorphism of the residues surrounding these sites; and (b) a recessed plate-like structure of the region containing these sites which hinders access by antibodies. On the other hand, HIV gp41 and SIV gp41 have various regions that are of low polymorphism and are suitably positioned on an exposed surface of the polypeptide (see below). Moreover, gp41 is involved in the infection process in that, following binding of the appropriate sites to CD4 and the chemokine receptor on a target cell, the complex composed of three gp120/gp41 units undergoes a conformational change which results in the insertion of the fusion peptide of gp41 into the host cell membrane. It is this latter step that facilitates entry of the virus into the target cell. Finally, in support of gp41's being a good candidate for HIV and SIV vaccine development, there are number of existing monoclonal antibodies specific for the membrane proximal gp41 ectodomain that neutralize across HIV clades.

Both natural and vaccine-induced immunity to malaria (caused by the protozoan parasites of the genus Plasmodium) have been hampered by antigenic variability of key immune molecules. Nevertheless, the ability of radiation-attenuated sporozoites to induce sterile protective immunity in murine and primate models (including man) and the ability of antibodies from semi-immune individuals to partially protect against infection clearly indicate the possibility of developing malaria-specific vaccines. As the blood stage of malaria is most responsible for clinical pathology and red blood cells lack major histocompatibility complex (MHC) class I and class II molecules, induction of antibody (rather than cytotoxic T lymphocyte) responses to blood stage antigens is key to establishing immunity to the parasite. Appropriate blood stage antigens of P. falciparum include merozoite surface protein-1 (MSP-1), ring-infected erythrocyte surface antigen (RESA), Plasmodium falciparum erythrocyte membrane protein-1 (PfFMP-1), Plasmodium falciparum 332 antigen (Pf332), Rosettin, merozoite surface protein-2 (MSP-2), serine stretch protein (SERP), glutamate-rich protein (GLURP), apical membrane antigen-1 (AMA-1), and histidine-rich protein-2 (HRP-2). Importantly, the presence of antibodies against MSP-1 and RESA (Pf155) has been to shown to correlate with protection from clinical episodes of malaria.

In regard to prostate cancer, PSMA is a good candidate for vaccine development since, unlike prostate specific antigen (PSA), it is not secreted but is expressed on the cell surface only, and selectively on the surface of tumor cells.

As used herein, an “active conformation” of a region of a PF is the conformation of the region, in terms of the number of molecular subunits and the three-dimensional structure, in the PF (or in the wild-type version of the PF where the PF is an altered form of a wild-type molecule) as it occurs in a pathogenic agent. Where the region exists in more than one conformation in the pathogenic agent, the active conformation of the region is the conformation of the region as it exists in the pathogenic agent prior to a pathogenesis-promoting activity of the pathogenic agent. Such pathogenesis-promoting activities include, for example, the insertion of all or part of a component of an infectious agent into a host cell membrane preliminary to entry of the infectious agent into the host cell. Another example of a pathogenesis-promoting activity is the binding of a pathogenic agent to a surface molecule of a mammalian cell preliminary to entry of the infectious agent into the cell. An additional pathogenesis-promoting activity can be the binding of a pathogenic agent (e.g., an infectious agent or a tumor cell) to a host component (e.g., a cell surface receptor or an extracellular matrix component) so as to facilitate homing of the pathogenic agent to a tissue or organ of the host. A specific example of such a pathogenesis-promoting activity is the insertion of HIV envelope glycoprotein (gp120/gp41 complex) into a host cell membrane, a step that follows binding of the HIV virion to CD4 on the host cell surface and appears to induce entry of the virus into the host cell.

In a PF region with “low polymorphism” (as used herein), there is little to no variability in structure between individuals of a particular species or type expressing the PF. Where the PF is a protein, this limited variability is reflected in a highly conserved amino acid sequence.

For example, in contrast to CD4- and chemokine-binding sites in HIV-1 gp120, HIV-1 gp41 has low polymorphism in that little variability is seen between the amino acid sequences of the gp41 regions of different HIV-1 clades or between individual virions in a subject infected with HIV-1. Similarly, a region of low polymorphism region in a PF of a breast cancer cell (or a cell of a class of breast cancer characterized by expression of the PF of interest) from a particular subject has essentially the same structure in: (a) breast cancer cells of other subjects with the same class of breast cancer; and (b) other breast cancer cells from the same subject.

One means of representing the polymorphism in a polypeptide is to determine the Shannon entropy for each amino acid in the polypeptide [Shannon, The mathematical theory of communication. University of Illinois Press: Urbana, Ill. (1949); Litwin et al. In, Theoretical and Experimental Insights into Immunology. Eds. Perelson, A.S. and Weisbuch, G. Springer-Verlag (1992); Stewart et al. (1997) Mol. Immunol. 34(15):1067-1082]. Multiple alleles or variants of the polypeptide of interest are compared and the Shannon entropy (H) for each residue is determined according to the formula: $H = {- {\sum\limits_{i = 1}^{i = 20}{p_{i}\quad\log_{2}p_{i}}}}$

-   -   where p_(i) is the fraction of residues (among the all the         variants/alleles compared) that are of amino acid type i.

For the 20 common amino acids, H can range from 0 (constant amino acid) to 4.32 (all amino acids represented equally). Sites at which H<2 are considered conserved and sites at which H>2 are considered not-conserved. By way of example, FIGS. 1A-B are bar charts showing (on the y-axis) the Shannon entropy for each amino acid residue as determined by comparing the amino acid sequences of HIV-1 gp41 ectodomains obtained from multiple mV-1 isolates from clades A (21 isolates; top chart), B (266 isolates; second chart), C (84 isolates; third chart) and O (10 isolates; fourth chart). The bottom chart (“ALL”) shows the data obtained when all the isolates (454) from all clades were compared. For this analysis, a region with low polymorphism (an “LP region”) is one containing nine or more consecutive residues, each having H≦1.3. The data shown for clades A and O should be treated with some caution since a rigorous Shannon entropy measure requires that a relatively high number of sequences (approximately 100) be compared. A consensus sequence for the relevant part of the polypeptide is shown below each row. As can be seen from FIG. 1; there are multiple regions of low variability.

However, low variability is not the only consideration in deciding upon a region of the molecule to focus on as a candidate for developing an immunogen of the invention. The region should be on an exposed surface of the protein and should preferably also neither contain nor be in close proximity to glycosylation sites on the polypeptide. LP regions may vary from one clade to another. In order to design a compound capable of eliciting a broad and general immune response, it is imperative to identify one or more LP regions that are common to all clades.

Thus, for example, the epitope recognized by the 2F5 monoclonal antibody (the boxed sequence (LDKWAS) (SEQ ID NO:5) towards the C-terminus of the C-domain of the ALL bar chart in FIG. 1B) would appear to be a good target for a cross-clade immunogenic response. However, a more careful inspection indicates that the 2F5 monoclonal antibody epitope is within a LP region for clades A and B (i.e., a region of nine or more amino acid residues, each residue having H≦1.3), but not for clades C and O since in these clades the residue at the fifth position of the 2F5 monoclonal antibody epitope has H>1.3.

For the purposes of the invention, a region of a protein with low polymorphism is a region containing at six or more (e.g., six, seven, eight, nine, ten, 11, 12, 13, 14, 15, 16, 18, 20, 24, 28, 35, 40, or more) consecutive amino acid residues, each amino acid residue having H≦2.0 (e.g., H≦1.8, ≦1.6, ≦1.4, ≦1.3, ≦1.2, ≦1.1, ≦1.0, ≦0.9, ≦0.8, ≦0.7, ≦0.6, ≦0.5, ≦0.4, ≦0.3, 0.2, or ≦0.1, or H=0). In view of the fact that they fulfill this criterion for low polymorphism and, in addition, are predicted to be on the surface of gp41 in its trimeric, preflusion state, a segment in the loop domain and a segment in the C-domain (or parts of the two segments or fragments containing either of the two segments) are promising candidates on which to perform the method of the invention. The amino acid sequences of these two segments in the consensus “ALL” chart (FIG. 1) are underlined and, in the “ALL” consensus sequence, the loop domain segment has the amino acid sequence LGIWGCSGKLICTT (SEQ ID NO:13) and the C-domain segment has the amino acid sequence SQNQQEKNEQELL (SEQ ID NO:14).

The PF used for designing immunogens can be purified from natural sources (e.g., from any of the pathogenic agents listed herein). Smaller peptides (fewer than 100 amino acids long) and other non-protein PF or compounds of the invention can be conveniently synthesized by standard chemical means known to those in the art. In addition, both polypeptides and peptides, either as PF or compounds of the invention, can be manufactured by standard in vitro recombinant DNA techniques and in Vihio transgenesis using nucleotide sequences encoding the appropriate polypeptides or peptides (see Nucleic Acids section below). Methods well-known to those skilled in the art can be used to construct expression vectors containing relevant coding sequences and appropriate transcriptional/translational control signals. See for example, the techniques described in Sambrook et al., Molecular Cloning: A Laboratory Manual (2nd Ed.) [Cold Spring Harbor Laboratory, N.Y., 1989], and Ausubel et al., Current Protocols in Molecular Biology [Green Publishing Associates and Wiley Interscience, N.Y., 1989].

For the methods of the invention, it is generally required that the PF or PF fragments be highly purified. Methods for purifying biological macromolecules (e.g., proteins) are known in the art. The degree of purity of a PF or PF fragment can be measured by any appropriate method, e.g., column chromatography, polyacrylamide gel electrophoresis, or BPLC analysis.

Nucleic Acids

The invention also includes nucleic acids encoding compounds of the invention (see below). In addition, nucleic acid molecules encoding PF can be useful for the invention. For example, they can be used for producing the PF in order to carry out the structural analyses described herein. The nucleic acid molecules can be cDNA, genomic DNA, synthetic DNA, or RNA, and can be double-stranded or single-stranded (i.e., either a sense or an antisense strand). Segments of these molecules are also considered within the scope of the invention, and can be produced by, for example, the polymerase chain reaction (PCR) or generated by treatment with one or more restriction endonucleases. A ribonucleic acid (RNA) molecule can be produced by in vitro transcription. Preferably, the nucleic acid molecules encode polypeptides that, regardless of length, are soluble under normal physiological conditions.

The nucleic acid molecules can contain naturally occurring sequences, or sequences that differ from those that occur naturally, but, due to the degeneracy of the genetic code, encode the same polypeptide. In addition, these nucleic acid molecules are not limited to coding sequences, e.g., they can include some or all of the non-coding sequences that lie upstream or downstream from a coding sequence.

The nucleic acid molecules can be synthesized (for example, by phosphoramidite-based synthesis) or obtained from a biological cell or infectious agent, such as a cell (e.g., a cancer cell) of a mammal or a virus.

In addition, the nucleic acid molecules of the invention, and those useful for the invention, include segments that are not found as such in the natural state. Thus, the invention encompasses recombinant nucleic acid molecules (for example, an isolated nucleic acid molecule encoding a compound of the invention) incorporated into a vector (for example, a plasmid or viral vector) or into the genome of a heterologous cell (or the genome of a homologous cell, at a position other than the natural chromosomal location). Recombinant nucleic acid molecules and uses therefor are discussed further below.

The invention also encompasses: (a) vectors (see below) that contain any of the sequences encoding the compounds of the invention; (b) expression vectors that contain any of the foregoing coding sequences operably linked to any transcriptional/translational regulatory elements (examples of which are given below) necessary to direct expression of the coding sequences; and (c) genetically engineered host cells (see below) that contain any of the foregoing expression vectors and thereby express the nucleic acid molecules of the invention.

The transcriptional/translational regulatory elements referred to above and further described below include but are not limited to inducible and non-inducible promoters, enhancers, operators and other elements that are known to those skilled in the art and that drive or otherwise regulate gene expression. Such regulatory elements include but are not limited to the cytomegalovirus hCMV immediate early gene, the early or late promoters of SV40 adenovirus, the lac system, the tr system, the TAC system, the TRC system, the major operator and promoter regions of phage A, the control regions of fd coat protein, the promoter for 3-phosphoglycerate kinase, the promoters of acid phosphatase, and the promoters of the yeast α-mating factors.

The expression systems that may be used for purposes of the invention include but are not limited to microorganisms such as bacteria (for example, E. coli and B. subtilis) transformed with recombinant bacteriophage DNA, plasmid DNA, or cosmid DNA expression vectors containing the nucleic acid molecules of the invention; yeast (for example, Saccharomyces and Pichia) transformed with recombinant yeast expression vectors containing the nucleic acid molecule of the invention; insect cell systems infected with recombinant virus expression vectors (for example, baculovirus) containing the nucleic acid molecule of the invention; plant cell systems infected with recombinant virus expression vectors (for example, cauliflower mosaic virus (CaMV) or tobacco mosaic virus (TMV)) or transformed with recombinant plasmid expression vectors (for example, Ti plasmid) containing a periostin nucleotide sequence; or mammalian cell systems (for example, COS, CHO, BHK, 293, VERO, HeLa, MDCK, WI38, and NIH 3T3 cells) harboring recombinant expression constructs containing promoters derived from the genome of mammalian cells (for example, the metallothionein promoter) or from mammalian viruses (for example, the adenovirus late promoter and the vaccinia virus 7.5K promoter). Also useful as host cells are primary or secondary cells obtained directly from a mammal and transfected with a plasmid vector or infected with a viral vector.

Cells transfected or transduced with the expression vectors of the invention can then be used, for example, for large or small scale in vitro manufacture of a polypeptide PF or compound of the. invention by methods known in the art. In essence, such methods involve culturing the cells under conditions that maximize production of the polypeptide and isolating the polypeptide from the cells or from the culture medium.

Data for Determining the 3-D Structure of a Molecule or Region of a Molecule

The 3-D structure of biological macromolecules (e.g., proteins, nucleic acids, carbohydrates, and lipids) can be determined from data obtained by a variety of methodologies. These methodologies, which have been applied most effectively to the assessment of the 3-D structure of proteins, include: (a) x-ray crystallography; (b) nuclear magnetic resonance (N1R) spectroscopy; (c) analysis of physical distance constraints formed between defined sites on a macromolecule, e.g., intramolecular chemical crosslinks between residues on a protein (e.g., International Patent Application No. PCT/US00/14667), and (d) molecular modeling methods based on a knowledge of the primary structure of a protein of interest, e.g., homology modeling techniques, threading algorithms, or ab initio structure modeling using computer programs such as MONSSTER (Modeling Of New Structures from Secondary and Tertiary Restraints) (see, e.g., International Application No. PCT/US99/11913). Other molecular modeling techniques may also be employed in accordance with this invention [e.g., Cohen et al. (1990) J. Med. Chem. 33: 883-894; Navia et al (1992) Current Opinions in Structural Biology, 2, pp. 202-210]. All these methods produce data that are amenable to computer analysis. Other spectroscopic methods that can also be useful in the method of the invention, but that do not currently provide atomic level structural detail about biomolecules, include circular dichroism and fluorescence and ultraviolet/visible light absorbance spectroscopy. A preferred method of analysis is x-ray crystallography. Descriptions of this procedure and of NMR spectroscopy are provided below.

X-ray Crystallogaphy

X-ray crystallography is based on the diffraction of x-radiation of a characteristic wavelength by electron clouds surrounding the atomic nuclei in a crystal of the PF region of interest. The technique uses crystals of purified biological macromolecules (but these frequently include solvent components, co-factors, substrates, or other ligands) to determine near atomic resolution of the atoms making up the particular biological macromolecule. A prerequisite for solving the 3-D structure of the macromolecule by x-ray crystallography -is a well-ordered crystal that will diffract x-rays strongly. The method directs a beam of x-rays onto a regular, repeating array of many identical molecules so that the x-rays are diffracted from the array in a pattern from which the structure of an individual molecule can be retrieved. Well-ordered crystals of, for example, globular protein molecules are large, spherical or ellipsoidal objects with irregular surfaces. The crystals contain large channels between the individual molecules. These channels, which normally occupy more than one half the volume of the crystal, are filled with disordered solvent molecules, and the protein molecules are in contact with each other at only a few small regions. This is one reason why structures of proteins in crystals are generally the same as those of proteins in solution.

Methods of obtaining the PF or PF fragments are described below. The formation of crystals is dependent on a number of different parameters, including pH, temperature, the concentration of the biological macromolecule, the nature of the solvent and precipitant, as well as the presence of added ions or ligands of the protein. Many routine crystallization experiments may be needed to screen all these parameters for the combinations that give a crystal suitable for x-ray diffraction analysis. Crystallization robots can automate and speed up work of reproducibly setting up a large number of crystallization experiments (see, e.g., Example 2 below and U.S. Pat. No. 5,790,421).

Polypeptide crystallization occurs in solutions in which the polypeptide concentration exceeds it's solubility maximum (i.e., the polypeptide solution is supersaturated). Such solutions may be restored to equilibrium by reducing the polypeptide concentration, preferably through precipitation of the polypeptide crystals. Often polypeptides may be induced to crystallize from supersaturated solutions by adding agents that alter the polypeptide surface charges or perturb the interaction between the polypeptide and bulk water to promote associations that lead to crystallization.

Crystallizations are generally carried out between 4° C. and 20° C. Substances known as “precipitants” are often used to decrease the solubility of the polypeptide in a concentrated solution by forming an energetically unfavorable precipitating depleted layer around the polypeptide molecules [Weber(1991]) Advances in Protein Chemistry, 41:1-36]. Inaddition to precipitants, other materials are sometimes added to the polypeptide crystallization solution. These include buffers to adjust the pH of the solution and salts to reduce the solubility of the polypeptide. Various precipitants are known in the art and include the following: ethanol, 3-ethyl-2-4 pentanediol, and many of the polyglycols, such as polyethylene glycol (PEG). The precipitating solutions can include, for example, 13-24% PEG 4000, 5-41% ammonium sulfate, and 1.0-1.5 M sodium chloride, and a pH ranging from 5-7.5. Other additives can include 0.1 M Hepes, 2-4% butanol, 0.1M or 20 mM sodium acetate, 50-70 mM citric acid, 120-130 mM sodium phosphate, 1 mM ethylene diamine tetraacetic acid (EDTA), and 1 mM dithiothreitol (DTT). These agents are prepared in buffers and are added dropwise in various combinations to the crystallization buffer.

Commonly used polypeptide crystallization methods include the following techniques: batch, hanging drop, seed initiation, and dialysis. In each of these methods, it is important to promote continued crystallization after nucleation by maintaining a supersaturated solution. In the batch method, polypeptide is mixed with precipitants to achieve supersaturation, and the vessel is sealed and set aside until crystals appear. In the dialysis method, polypeptide is retained in a sealed dialysis membrane that is placed into a solution containing precipitant. Equilibration across the membrane increases the polypeptide and precipitant concentrations, thereby causing the polypeptide to reach supersaturation levels.

In the preferred hanging drop technique [McPherson (1976) J. Biol. Chem., 251:6300-6306], an initial polypeptide mixture is created by adding a precipitant to a concentrated polypeptide solution. The concentrations of the polypeptide and precipitants are such that in this initial form, the polypeptide does not crystallize. A small drop of this mixture is placed on a glass slide that is inverted and suspended over a reservoir of a second solution. The system is then sealed. Typically, the second solution contains a higher concentration of precipitant or other dehydrating agent. The difference in the precipitant concentrations causes the protein solution to have a higher vapor pressure than the second solution. Since the system containing the two solutions is sealed, an equilibrium is established, and water from the polypeptide mixture transfers to the second solution. This equilibrium increases the polypeptide and precipitant concentration in the polypeptide solution. At the critical concentration of polypeptide and precipitant, a crystal of the polypeptide may form.

Another method of crystallization introduces a nucleation site into a concentrated polypeptide solution. Generally, a concentrated polypeptide solution is prepared and a seed crystal of the polypeptide is introduced into this solution. If the concentrations of the polypeptide and any precipitants are correct, the seed crystal will provide a nucleation site around which a larger crystal forms.

Yet another method of crystallization is an electrocrystallization method in which use is made of the dipole moments of protein macromolecules that self-align in the Helmholtz layer adjacent to an electrode (see U.S. Pat. No. 5,597,457).

Some proteins may be recalcitrant to crystallization. However, several techniques are available to the skilled artisan to induce crystallization. For example, the removal of flexible polypeptide segments at the amino or carboxyl terminal end of the protein may facilitate production of crystalline protein samples. Removal of such segments can be done using molecular biology techniques or treatment of the protein with proteases such as trypsin, chymotrypsin, or subtilisin.

In diffraction experiments, a narrow and parallel beam of x-rays is taken from the x-ray source and directed onto the crystal to produce diffracted beams. The incident primary beams cause damage to both the macromolecule and solvent molecules. The crystal is, therefore, cooled (e.g., to −220° C. to −50° C.) to prolong its lifetime. The primary beam must strike the crystal from many directions to produce all possible diffraction spots, so the crystal is rotated in the beam during the experiment. The diffracted spots are recorded on a film or by an electronic detector. Exposed film has to be digitized and quantified in a scanning device, whereas the electronic detectors feed the signals they detect directly into a computer. Electronic area detectors significantly reduce the time required to collect and measure diffraction data. Each diffraction beam, which is recorded as a spot on film, is defined by three properties: the amplitude, which is measured from the intensity of the spot; the wavelength, which is set by the x-ray source; and the phase, which is lost in x-ray experiments. All three properties are needed for all of the diffracted beams in order to determine the positions of the atoms giving rise to the diffracted beams. One way of determining the phases is called Multiple Isomorphous Replacement (MIR), which requires the introduction of exogenous x-ray scatterers (e.g., heavy atoms such metal atoms) into the unit cell of the crystal. For a more detailed description of MIR, see U.S. Pat. No. 6,093,573, column 15.

Atomic coordinates refer to Cartesian coordinates (x, y, and z positions) derived from mathematical equations involving Fourier synthesis of data derived from patterns obtained via diffraction of a monochromatic beam of x-rays by the atoms (scattering centers) of biological macromolecule of interest in crystal form. Diffraction data are used to calculate electron density maps of repeating units in the crystal (unit cell). Electron density maps are used to establish the positions (atomic coordinates) of individual atoms within a crystal's unit cell. The absolute values of atomic coordinates convey spatial relationships between atoms because the absolute values ascribed to atomic coordinates can be changed by rotational and/or translational movement along x, y, and/or z axes, together or separately, while maintaining the same relative spatial relationships among atoms. Thus, a biological macromolecule (e.g., a protein) whose set of absolute atomic coordinate values can be rotationally or translationally adjusted to coincide with a set of prior determined values from an analysis of another sample is considered to have the same atomic coordinates as those obtained from the other sample.

Further details on x-ray crystallography can be obtained from U.S. Pat. No. 6,093,573 and International Application Nos. PCT/US99/18441, PCT/US99/11913, and PCT/US00/03745.

NMR Spectroscopy

While x-ray crystallography requires single crystals of a macromolecule of interest, NMR measurements are carried out in solution under near physiological conditions. However, NMR-derived structures are not as detailed as crystal-derived structures.

While the use of No spectroscopy was until relatively recently limited to the elucidation of the 3-D structure of relatively small molecules (e.g., proteins of 100-150 amino acid residues), recent advances including isotopic labeling of the molecule of interest and transverse relaxation-optimized spectroscopy (TROSY) have allowed the methodology to be extended to the analysis of much larger molecules, e.g., proteins with a molecular weight of 110 IkDa [Wider (2000) BioTechniques, 29:1278-1294].

NMR uses radio-frequency radiation to examine the environment of magnetic atomic nuclei in a homogeneous magnetic field pulsed with a specific radio frequency. The pulses perturb the nuclear magnetization of those atoms with nuclei of nonzero spin. Transient time domain signals are detected as the system returns to equilibrium. Fourier transformation of the transient signal into a frequency domain yields a one-dimensional NMR spectrum. Peaks in these spectra represent chemical shifts of the various active nuclei. The chemical shift of an atom is determined by its local electronic environment. Two-dimensional NMR experiments can provide information about the proximity of various atoms in the structure and in three dimensional space. Protein structures can be determined by performing a number of two- (and sometimes 3- or 4-) dimensional NMR experiments and using the resulting information as constraints in a series of protein folding simulations.

More information on NoM spectroscopy including detailed descriptions of how raw data obtained from an NMR experiment can be used to determine the 3-D structure of a macromolecule can be found in: Protein NMR Spectroscopy, Principles and Practice, J. Cavanagh et al., Academic Press, San Diego, 1996; Gronenborn et al. (1990) Anal. Chem. 62(1):2-15; and Wider (2000), supra.

Any available method can be used to construct a 3-D model of a PF region of interest from the x-ray crystallographic and/or NMR data using a computer as described above. Such a model can be constructed from analytical data points inputted into the computer by an input device and by means of a processor using known software packages, e.g., HIL, MOSFILM, XDS, CCP4, SHARP, PHASES, HEAVY, XPLOR, TNT, NMRCOMPASS, NMRPIPE, DIANA, NMRDRAW, FELIX, VN, MADIGRAS, QUANTA, BUSTER, SOLVE, O, FRODO, or CHAIN. The model constructed from these data can be visualized via an output device of a computer, using available systems, e.g., Silicon Graphics, Evans and Sutherland, SUN, Hewlett Packard, Apple Macintosh, DEC, IBM, or Compaq.

Designing Compounds of the Invention

Once the 3-D structure of a PF region of interest has been established using any of the above methods, a compound that has substantially the same 3-D structure (or contains a domain that has substantially the same structure) as the relevant PF region can be made. In this context, “has substantially the same 3-D structure” means that the compound includes one or more (e.g., one, two, three, four, five, six, seven, eight, nine, ten, 12, 15, 20, 30, 40, 50, 100, or more) epitopes with the ability to induce the production in a mammal (e.g., a human, non-human primate (e.g., a monkey or a chimpanzee), horse, cow, sheep, goat, pig, cat, dog, rabbit, guinea pig, rat, hamster, or mouse) of an antibody that binds to the region of the PF in its active conformation. One of skill in the art would know how to test a compound for such an ability.

With the above described 3-D structural data on hand and knowing the chemical structure (e.g., amino acid sequence in the case of a protein) of the PF region of interest, those of skill in the art would know how to make compounds with the above-described properties. Such methods include chemical synthetic methods and, in the case of proteins, recombinant methods (see above). For example, cysteine residues appropriately placed in a compound so as to form disulfide bonds can be used to constrain the compound or a domain of the compound in an appropriate 3-D structure. In addition, in a compound that is a polypeptide or includes a domain that is a polypeptide, one of skill in the art would know what amino acids to include and in what sequence to include them in order to generate, for example, α-helices, β structures, or sharp turns or bends in the polypeptide backbone.

While not essential, computer-based methods can be used to design the compounds of the invention. Appropriate computer programs include: LUDI (Biosym Technologies, Inc., San Diego, Calif.), Aladdin (Daylight Chemical Information Systems, Irvine, Calif.); and LEGEND [Nishibata et al. (1985) J. Med. Chem. 36(20):2921-2928].

The compounds of the invention can include, in addition, to the above described immunogenic domains, one or more domains that facilitate purification (e.g., poly-histidine sequences) or domains that serve to direct the compound to organs of the immune system, e.g., ligands or antibodies (including antibody fragments such Fab, F(ab′)₂, or single chain Fv fragments) specific for cell surface components of cells of the immune system, e.g., the F1t3 ligand or antibodies specific for CD4, CD8, CD3, CD2, CD19, or CD20. Other useful domains include immune stimulatory cytokines (e.g., without limitation, interleukin (IL)-2, IL4, IL-5, IL-6, IL-10, IL-13), adjuvant molecules (e.g., cholera toxin or E. coli heat labile toxin) or functional fragments of such molecules, i.e., those retaining at least some, e.g., 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, or all, of the activity of the parent molecule, or at least the receptor-binding activity. All that is required in such multidomain compounds is that the immunogenic domain retains the 3-D structure it would have in the absence of the additional domains. Conjugation to make such multidomain compounds can be by chemical methods (e.g., Barrios et al. (1992) Eur. J. Immunol. 22:1365-1372]. Where the compound is a peptide, it can be produced as part of a recombinant protein, such as one that self-assembles into virus-sized particles (e.g., U.S. Pat. No. 4,918,166) that display the immunogenic peptide on the surface.

Compounds of the invention that are peptides also include those described above, but modified for in vivo use by the addition, at the amino- and/or carboxyl-terminal ends, of a blocking agent to facilitate survival of the relevant polypeptide in vivo. This can be useful in those situations in which the peptide termini tend to be degraded by proteases prior to cellular uptake. Such blocking agents can include, without limitation, additional related or unrelated peptide sequences that can be attached to the amino and/or carboxyl terminal residues of the peptide to be administered. This can be done either chemically during the synthesis of the peptide or by recombinant DNA technology by methods familiar to artisans of average skill.

Alternatively, blocking agents such as pyroglutamic acid or other molecules known in the art can be attached to the amino and/or carboxyl terminal residues, or the amino group at the amino terminus or carboxyl group at the carboxyl terminus can be replaced with a different moiety. Likewise, the peptide compounds can be covalently or noncovalently coupled to pharmaceutically acceptable “carrier” proteins prior to administration.

Also of interest are peptidomimetic compounds that are designed based upon the amino acid sequences of compounds of the invention that are peptides. Peptidomimetic compounds are synthetic compounds having a three-dimensional conformation (i.e., a “peptide motif”) that is substantially the same as the three-dimensional conformation of a selected peptide. The peptide motif provides the peptidomimetic compound with the ability to elicit the production of antibodies cross-reactive with a selected peptide. Peptidomimetic compounds can have additional characteristics that enhance their ill vivo utility, such as increased cell permeability and prolonged biological half-life.

The peptidomimetics typically have a backbone that is partially or completely non-peptide, but with side groups that are identical to the side groups of the amino acid residues that occur in the peptide on which the peptidomimetic is based. Several types of chemical bonds, e.g., ester, thioester, thioamide, retroamide, reduced carbonyl, dimethylene and ketomethylene bonds, are known in the art to be generally useful substitutes for peptide bonds in the construction of protease-resistant peptidomimetics.

Determining the Immunogenicity of the Compounds of the Invention

A candidate compound can be tested for immunogenicity by any of a number of methods known in the art. For example, the test compound can administered to a test mammal (e.g., a human patient or volunteer, non-human primate (e.g., a monkey or a chimpanzee), horse, cow, sheep, goat, pig, cat, dog, rabbit, guinea pig, rat, hamster, or mouse). The test compound can be administered orally or transdermally, or injected (or infused) intravenously, subcutaneously, intramuscularly, intraperitoneally, intrarectally, intravaginally, intranasally, intragastrically, intratracheally, or intrapulmonarily. They can be delivered directly to an appropriate lymphoid tissue (e.g. spleen, lymph node, or mucosal-associated lymphoid tissue (MALT)). The test substance could be administered alone or with adjuvant, e.g., cholera toxin (CT), E. coli heat labile toxin (LT), mutant CT (MCT) [Yamamoto et al. (1997) J. Exp. Med. 185:1203-1210] and mutant E. coli heat labile toxin (MLT) (Di Tommaso et al. (1996) Infect. Immunity 64:974-979]. MCT and MLT contain point mutations that substantially diminish toxicity without substantially compromising adjuvant activity relative to that of the parent molecules. Other useful adjuvants include alum, Freund's complete and incomplete adjuvant, and RIBI. If desired, booster immunizations may be given once or several (two, three, four, eight or twelve, for example) times at various times (e.g., spaced one week apart). Antibody (e.g., IgG, IgM, or IgA) responses specific for the compound and/or for the PF from which the compound was derived can then be measured by testing for the presence of such antibodies systemically (e.g., in serum) or, for example, at various mucosal sites (e.g., in saliva or gastric and bronchoalveolar lavages) using in vitro assays familiar to those in the art, e.g., the enzyme-linked immunosorbent assay (ELISA). Alternatively, or in addition, since CD4+ T cell responses are generally required for antibody responses, in vitro CD4+ T cell responses to the test compound and/or the relevant PF can be measured using methods known in the art. Such methods include CD4+ T cell proliferation or lymphokine (e.g., interleukin-2, interleukin4, or interferon-γ) production assays. In addition, in vivo skin tests can be performed on the test mammals. Such assays test for the both antibodies and pre-activated CD4+ T cells specific for the test antigen. A positive response within 12 hours is indicative of an antibody response while a response that is optimal between 48 and 96 hours indicates the presence of CD4+ T cells that have previously been exposed to the relevant antigen.

The same or identically treated mammals can also be tested for resistance to infection by a relevant infectious agent or for tumor development after injection or implantation of appropriate tumor cells. After immunization (as indicated above), the test mammals are injected or implanted with a single dose or various doses of the relevant infectious agent or tumor cells. The test mammals can be observed for pathologic symptoms familiar to those in the art, e.g, malaise, lack of appetite, morbidity and mortality. Alternatively, they may euthanized at various time points and their tissues (e.g., lung, liver, spleen, kidney or intestine) may be assayed for relative levels of the infectious agent or tumor cells by methods known to artisans of ordinary skill (e.g., viral plaque forming assays or immunocytochemical assays using antibodies specific for tumor cell markers). The data obtained with the test mammals can be compared to those obtained with a control group of mammals, e.g., mammals that were exposed to the diluent in which the test compound was dissolved or suspended (e.g. physiological saline) or adjuvant without the compound if adjuvant was used for immunization. Increased resistance of the test mammals to infection or tumor development, relative to the control mammals, would indicate that the test compound is an effective vaccine.

In vitro neutralization assays (e.g., see Example 4 below) familiar to those in the art can also be performed to test for the presence of infectious agent-specific neutralizing antibodies in samples (e.g., serum samples) obtained from the above described test and control mammals. In addition, sera from test and control subjects can be tested for the presence of antibodies that can kill tumor cells by, for example, complement-mediated lysis or antibody dependent cell-mediated cytotoxicity (ADCC) by methods known to those skilled in the art.

Methods of Activating an Immune Response

The invention features methods of activating mammalian immune responses in which cells of the immune system are exposed to one or more compounds of the invention.

The methods of the invention can be performed in vitro or in vivo. In vitro application of the compounds of the invention can be useful, for example, in basic scientific studies of immune mechanisms or for the production of antibodies, e.g., for use in studies on infection or cancer or for passive immunotherapy. In vitro activation with the compounds of the invention can also be used to obtain activated B lymphocytes useful for deriving monoclonal antibody-producing cell lines (e.g., human antibody-producing cell lines or hybridomas).

In the in vitro methods of the invention, lymphoid cells (including T and B lymphocytes) obtained from a mammalian subject are cultured with a compound of the invention. The lymphoid cells can be from a subject pre-exposed to the compound, to the PF from which the compound was derived, or to a pathogenic agent that produces the PF; alternatively, the donor of the lymphoid cells need not have been exposed to any of these entities. The cultures can be “restimulated” as often as necessary with either the compound or the PF. The cultures can also be monitored at various times to ascertain whether the desired level of immune reactivity (e.g., antibody production or CD4+ T cell activity) has been attained.

The compounds of the invention are generally useful for generating immune responses and as prophylactic vaccines or immune response-stimulating therapeutics. Thus, the responses elicited by the compounds need have neither prophylactic nor therapeutic efficacy. They can be used, for example, (a) to elicit large-quantities of antibodies in mammals (e.g., rabbits, goats, sheep, or horses) that are subsequently isolated from the animals and used for purposes such as antigen detection or purification, or (b) for immunization of animals (e.g., mice, rats, or hamsters) with a view to making monoclonal antibodies.

The compounds can also be used, for example, as vaccines or therapeutic agents against (a) infectious diseases due to any of the infectious agents listed herein; or (b) cancers such as any of those listed herein. The compounds can be useful in the prevention and/or therapy of diseases involving intracellular microorganisms (i.e., infectious agents that replicate inside a cell), e.g., viruses such as influenza virus or HIV, intracellular bacteria such M. tuberculosis, and intracellular protozoans such as P. falcipartim or any of the other infectious agents listed herein. In addition, the compounds can be useful therapeutics for cancer (e.g., any of those recited above); in cases where a subject is at relatively high risk for a cancer (e.g., prostate cancer in men over 50 years of age, lung cancer in a tobacco smoker, or melanoma in a subject with multiple nevi), appropriate compounds can be used as prophylactic vaccines.

As used herein, “prophylaxis” can mean complete prevention of the symptoms of a disease, a delay in onset of the symptoms of a disease, or a lessening in the severity of subsequently developed disease symptoms. “Prevention” should mean that symptoms of the disease (e.g., an infection) are essentially absent. As used herein, “therapy” can mean a complete abolishment of the symptoms of a disease or a decrease in the severity of the symptoms of the disease. As used herein, a “protective” immune response is an immune response that is prophylactic and/or therapeutic.

The methods of the invention can be applied to a wide range of species, e.g., humans, non-human primates (e.g., monkeys), horses, cattle, pigs, sheep, goats, dogs, cats, rabbits, guinea pigs, hamsters, rats, and mice.

In one in vivo approach, the compound itself is administered to the subject. Generally, the compounds of the invention will be suspended in a pharmaceutically-acceptable carrier (e.g., physiological saline) and administered orally or transdermally or injected (or infused) intravenously, subcutaneously, intramuscularly, intraperitoneally, intrarectally, intravaginally, intranasally, intragastrically, intratracheally, or intrapulmonarily. They can be delivered directly to an appropriate lymphoid tissue (e.g. spleen, lymph node, or mucosal-associated lymphoid tissue (MALT)). A live cell vector containing a DNA encoding (a) the peptide compound or (b) a fusion protein containing the peptide compound, can be delivered orally or directly to the MALT. The dosage required depends on the route of administration, the nature of the formulation, the nature of the patient's illness, the subject's size, weight, surface area, age, and sex, other drugs being administered, and the judgment of the attending physician. Suitable dosages are in the range of 0.001-100.0 mg/kg. Wide variations in the needed dosage are to be expected in view of the variety of compounds available and the differing efficiencies of various routes of administration. For example, oral administration would be expected to require higher dosages than administration by intravenous injection. Variations in these dosage levels can be adjusted using standard empirical routines for optimization, as is well understood in the art.

Administrations can be single or multiple (e.g., 2- or 3-, 4-, 6-, 8-, 10-, 20-, 50-, 100-, 150-, or more fold). Encapsulation of the compounds in a suitable delivery vehicle (e.g., polymeric microparticles or implantable devices) may increase the efficiency of delivery, particularly for oral delivery. The frequency of administration can be as indicated above in the section describing method for determining the immunogenicity of the compounds of the invention. In addition, the same adjuvants described in that section can be used.

Alternatively, a polynucleotide containing a nucleic acid sequence encoding a compound of interest can be delivered to an appropriate cell of the animal. Expression of the coding sequence will preferably be directed to lymphoid tissue of the subject by, for example, delivery of the polynucleotide to the lymphoid tissue. This can be achieved by, for example, the use of a polymeric, biodegradable microparticle or microcapsule delivery vehicle, sized to optimize phagocytosis by phagocytic cells such as macrophages. For example, PLGA (poly-lacto-co-glycolide) microparticles approximately 1-10 μm in diameter can be used. The polynucleotide is encapsulated in these microparticles, which are taken up by macrophages and gradually biodegraded within the cell, thereby releasing the polynucleotide. Once released, the DNA is expressed within the cell. A second type of microparticle is intended not to be taken up directly by cells, but rather to serve primarily as a slow-release reservoir of nucleic acid that is taken up by cells only upon release from the micro-particle through biodegradation. These polymeric particles should therefore be large enough to preclude phagocytosis (i.e., larger than 5μm and preferably larger than 20μm).

Another way to achieve uptake of the nucleic acid is using liposomes, prepared by standard methods. The vectors can be incorporated alone into these delivery vehicles or co-incorporated with tissue-specific antibodies. Alternatively, one can prepare a molecular conjugate composed of a plasmid or other vector attached to poly-L-lysine by electrostatic or covalent forces. Poly-L-lysine binds to a ligand that can bind to a receptor on target cells [Cristiano et al. (1995), J. Mol. Med. 73, 479]. Alternatively, lymphoid tissue specific targeting can be achieved by the use of lymphoid tissue-specific transcriptional regulatory elements (TRE) such as a B lymphocyte, T lymphocyte, or dendritic cell specific TRE. Lymphoid tissue specific TRE are known [Thompson et al. (1992), Mol. Cell. Biol. 12, 1043-1053; Todd et al. (1993), J. Exp. Med. 177, 1663-1674; Penix et al. (1993), J. Exp. Med. 178, 1483-1496]. Delivery of “naked DNA” (i.e., without a delivery vehicle) to an intramuscular, intradermal, or subcutaneous site is another means to achieve in vivo expression.

In the relevant polynucleotides (e.g., expression vectors) the nucleic acid sequence encoding the compound with an initiator methionine and optionally a targeting sequence is operatively linked to a promoter or enhancer-promoter combination. Promoters and enhancers are described above.

Polynucleotides can be administered in a pharmaceutically acceptable carrier. Pharmaceutically acceptable carriers are biologically compatible vehicles which are suitable for administration to a human or other mammalian subject, e.g., physiological saline. A therapeutically effective amount is an amount of the polynucleotide that is capable of producing a medically desirable result (e.g., an antibody response) in a treated animal. As is well known in the medical arts, the dosage for any one patient depends upon many factors, including the patient's size, body surface area, age, the particular compound to be administered, sex, time and route of administration, general health, and other drugs being administered concurrently. Dosages will vary, but a preferred dosage for administration of polynucleotide is from approximately 10⁶ to 10¹² copies of the polynucleotide molecule. This dose can be repeatedly administered, as needed. Routes and frequency of administration can be any of those listed above.

These methods of the invention can be applied to any of the diseases and species listed here. Methods to test whether a compound is therapeutic for or prophylactic against a particular disease are known in the art. Where a therapeutic effect is being tested, a test population displaying symptoms of the disease (e.g., cancer patients) is treated with a test compound of the invention, using any of the above described strategies. A control population, also displaying symptoms of the disease, is treated, using the same methodology, with a placebo. Disappearance or a decrease of the disease symptoms in the test subjects would indicate that the compound was an effective therapeutic agent.

By applying the same strategies to subjects prior to onset of disease symptoms (e.g., presymptomatic subjects considered to likely candidates for cancer development (see above) or experimental animals in which an appropriate disease spontaneously arises or can be deliberately induced, e.g., multiple murine cancers), the compounds can be tested for efficacy as prophylactic agents, i.e., vaccines. In this situation, prevention of onset of disease symptoms is tested. Analogous strategies can be used to test for the efficacy of the compounds in the prophylaxis of a wide variety of infectious diseases, e.g., those involving any of the microorganisms listed above.

The following examples are meant to illustrate, not limit, the invention.

EXAMPLES

The following examples describe experiments designed to generate an SIV-specific immunogen based on the 3-D structure of the ectodomains of SIV gp41 as they exist in the gp120/gp41 trimer prior to binding to CD4 and a chemokine receptor on appropriate target cells. An x-ray crystallographic analysis is performed on a trimer of SIV gp140 rather than a trimer of the g120/gp41 complex. SIV gp41 is a recombinant form of the ectodornains of SIV gp160in which the primary and secondary cleavage sites between gp120 and gp41 are mutated to prevent cleavage into gp120 and the ectodomains of gp41. Recent results of chemical cross-linking, analytical ultracentrifugation, and mass spectrometry experiments indicate that secreted recombinant gp140is, like wild-type gp120/gp41, a trimer [Chen et al. (2000) J. Biol.Chem. 45(10):34946-34953] The 3-D structure of gp41 in trimers of gp140is likely to be substantially the same as in trimers of gp120/gp41 because gp41-specific antibodies that are conformationally specific (i.e., that do not bind to denatured gp41) bind to trimers of both gp140 and gp120/gp41.

Example 1

Production of Recombinant SIV gp140 Production of SIV gp140in Mammalian Cells

SIV gp140from the SIV strain Mac23H pJ5 [Rud et al. Iii, Vaccines 92: Modern Approaches to New Vaccines Including Prevention of AIDS (Brown, F., Chanock, R. M., Ginsberg, H. S., and-Lerner, R. A., eds) pp. 229-235, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 1992] was expressed in CHO-Lec3.2.8.1 cells using an expression construct (pGP140) that was the same as pSIV-M [Rhodes et al. (1994) J. Gen. Virol. 75:207-213] but a shorter heterologous tissue plasminogen activator (tpA) leader sequence was used. The cDNA sequence (SEQ ID NO:1) encoding Mac23HpJ25 gp160 is shown in FIG. 2A and the amino acid sequence (SEQ ID NO:2) of Mac23HpJ25 gp160, including the leader peptide, is shown in FIG. 2B. The site at which the leader peptide is cleaved is indicated by a vertical line. In FIG. 3A is shown the cDNA sequence (SEQ ID NO:3) encoding gp140in pGP140, including the heterologous tPA leader peptide. In FIG. 3B is shown the amino acid sequence (SEQ ID NO:4) of gp140, including the tPA leader peptide. The site at which the leader peptide is cleaved is indicated by a vertical line. Note that the two basic residues at the primary cleavage site (Lys-523) and a secondary cleavage site (Arg-512) between gp120 and gp41 of the Mac23HpJ5 gp160 have been replaced by glutamic acid residues to prevent cleavage of the gp140 molecule and to avoid shedding of gp120that is observed with native constructs.

In brief, 20 μg of Sall-linearized pGP140 DNAwas transfected into Lec3.2.8.1 cells by calcium phosphate precipitation. Transformants were selected in GMEM medium (Life Technologies. Inc., Carlsbad, Calif.) containing 25 μM methionine sulfoximine and assayed for secretion of soluble SIV gp140 by enzyme-linked immunosorbent assays (ELISA). Immulonr plates (Dynatech Laboratories, Inc., Chantilly, Va.) were coated with anti-SIV ENV monoclonal antibody KK19 [Kent et al. (1991) Aids 5:829-836] by incubating the wells ofthe plates with a 4 μg/ml solution of the antibody overnight at 4° C.; non-specific protein binding sites in the wells were blocked with 1% solution of bovine serum albumin (BSA) in phosphate buffered saline (PBS) at room temperature for 2 hours. Cell culture supernatant (50 μl per well) from each transformant clone was added to the wells of the plates, which were incubated overnight at 4° C. The plates were washed with PBS containing 0.1% BSA and incubated with biotinylated anti-SIV ENV monoclonal antibody KK41 (0.2 μg/ml) [Kent et al. (1992) AIDS Res. Hum. Retroviruses 8:1147-1151] for 2 hours at room temperature. After washing again, the plates were developed with horseradish peroxidase-conjugated streptavidin (Sigma, St. Louis, Mo.). The highest expressing cells were chosen for rescreening with the same assay. The expression of gp140 was also confirmed by immunoprecipitation. Large scale production of SIV gp140 was carried out following a protocol previously described [Liu et al. (1996) J. Biol Chem. 271:33639-33646] in 175 cm² tissue culture flasks or 850 cm² roller bottles (Corning, Oneonta, N.Y.).

Production of SIV gp140 in Insect Cells

The pFBSIV-His1 expression vector was constructed to express SIV gp140 in insect cells using the Bac-to-Bac expression system (Life Technologies, Inc.). The polypeptide produced by pFBSIV-His1includes gp140, the honey bee melittin secretion signal sequence at the N-terminus of gp140, and a hexahistadine sequence at the N-terminus of gp140 to facilitate purification by Nickel affinity chromatography. The coding sequence in pSIV-M was amplified by PCR using primers IG1 (5′-CGCGGATCCGACTCAATATGTCACAGTCTTTTAT-3′) (SEQ ED NO:6) and IG2 (5′-GGCCGAATTCTATATCCAAGAAGCAAGG-3′) (SEQ ID NO:7) to produce a DNA fragment encompassing the complete SIV gp140 coding sequence. The PCR product was digested with BamHI and EcoRI, gel-purified, and cloned into pMelBac (Invitrogen) to generate an intermediate construct pBacSIV-5, which was sequenced using primers to verify the entire sequence of SIV gp140open reading frame. The coding sequence in pBacSIV-5 was then amplified using primers IG3 (5 ′-TTTATGGTCGTATACATTTCTTACATCTATGCGACTCAATATGTCACAGTC-3′) (SEQ ID NO:8) and IG4 (5′-TAGTCTCATTGACCATGTCT-3′) (SEQ ID NO:9). The resulting PCR product was reamplified using primers IG5 (5′-CGCGGATCCATGAAATTCTTAGTCAACGTTGCCCTTGTTTTTATGGTC GTATACATT-3′) (SEQ ID NO:10) and IG4 to produce a 447-bp fragment, which was digested with BamnHI and NsiI, gel-purified, and designated as fragment 1. This fragment allows fusion of the N terminus of SIV gp140 and the melittin secretion signal sequence. pBacSIV-5 was digested with NsiI and NcoI and a 1.5-kb fragment (designated fragment 2), which encompassed a major portion of SIV gp140 open reading frame, was gel-purified. To introduce a histidine tag at the C-terminus of SIV gp140, a 757-bp PCR product was amplified using pBacSIV-5 as template and IG6 (5′-GAGACCTCACGTGTAACT-3′) (SEQ ID NO:11) and IG7 (5′-CCGGAATTCTCAATGATGATGATGATGATGAGTGCGACCTTCGATTTGTATA TACTTATCCAAGA-3′) (SEQ ID NO:12) as primers and digested with NcoI and EcoRl, gel-purified, and designated as fragment 3. Fragments 1, 2, and 3 were ligated together and cloned into pFastBac-1 (Life Technologies, Inc.), digested with BamHI and EcoRI, to give the expression construct pFBSIV-His1.

Recombinant baculovirus was generated according to the manufacturer's protocol and amplified in Sf9 insect cells in TNM-FH medium (Sigma). Expression of SIV gp140 was confirmed by a Western blot using sheep antisera against SIV envelope glycoprotein. The optimal amount of virus and postinfection harvest time was determined by small scale tests in 100-ml spinner flasks. Infected Trichoplusia ni (Hi-5) cells were found to secrete significantly more SIV gp140than Sf9 cells as assessed by Western blotting. For large scale protein production, 10 liters of T. ni (Hi-5) cells (2×106 cells/ml) in Ex-Cell 405 medium (JRH Biosciences) were infected at a multiplicity of infection of 2.5. Three days after infection, the supernatant was harvested by centrifugation and concentrated to 1 liter in a tangential flow filtration system, ProFlux M 12 (Millipore Corp.).

Purification of SIV gp140

The CHO Lec3.2.8.1 transfectant supernatants containing secreted SIV gp140 were harvested by centrifugation or by filtration through a Coming filter (0.22 mm). SIV gp140 was purified by an immunoaffinity chromatography using a mAb 17A11 affinity column (5-ml bed volume), where the monoclonal antibody 17A11 was cross-linked at 5 mg/ml to GammaBind™ Plus Sepharose (Amersham Pharmacia Biotech, Piscataway, N.J.) with dimethyl pimelimidate (Pierce Chemical Co., Rockford, Ill.). The supernatants were passed through the column with a flow rate of about 0.5 ml/min. After extensive washing with PBS the protein was eluted with 100 mM glycine (pH 3.0), followed by immediate neutralization with 2 M Tris-HCI (pH 8.0) and 150 mM NaCl.

SIV gp140 expressed from insect cells was purified by metal chelate affinity chromatography with ProBondrm resin (Invitrogen, Carlsbad, Calif.). Concentrated insect cell culture supernatants were immediately exchanged into 1X column buffer (25 mM sodium phosphate (pH 8.0), 250 mM NaCI) in a ProFlux M 12 flow filtration system to remove small molecules in the medium that interfere with the binding of His-tagged SIV gp140 to the nickel column. After centrifugation at 5000 rpm in a JA-14 rotor (Beckman, Fullerton, Calif.) for 15 minutes to remove insoluble materials, imidazole was added to a final concentration of 15 mM to reduce nonspecific binding to the resin. Batch binding was then performed at 4° C. for 3 hours. After packing the column (about 5-ml bed volume), the beads were washed by 100 ml of 1X column buffer containing 15 mM imidazole, followed by further washing with 50 ml of 40 mM imidazole in 1X column buffer. The protein was eluted with 300 mM imidazole in 1X column buffer. The fractions were analyzed by SDS-PAGE. The fractions containing SIV gp140 were pooled, concentrated, and further purified by gel filtration chromatography on Superdex 200 or Superose 6™(Amersham Pharmacia Biotech) with a buffer containing 25 mM Tris-HCl and 150 mM NaCl.

Production of SIV gp40 in Bacteria

cDNA encoding SIV gp140 is cloned into a bacterial expression vector, e.g., pET 11a. For bacterial expression, the resulting construct is transformed into E. coli strain BL21 (DE3) bacteria carrying a chromosomal copy of T7 RNA polymerase under control of the IPTG inducible lac promoter. An overnight preculture of a transformant colony in 10 ml of Luria both medium supplemented with ampicillin (0.1 mg/ml) is inoculated into 1 liter of Luria broth medium at 37° C. and the culture is grown to log phase. Overproduction of the protein is initiated by addition of IPTG (isopropyl-β-D-thiogalactopyranoside) to a final concentration of 1 mM. After a further 3 hour incubation, the cells are harvested by centrifugation and then lysed by sonication. The isolated inclusion bodies are solubilized with buffer A (0.2M Tris-HCI pH 9.5, 6M guanidinium-HCl, 0. IM DTT and 1 mM EDTA) overnight at 4° C. and the resulting solution is dialyzed with buffer A without DTT at 4° C. Refolding of gp140is done by rapid dilution to a final protein concentration of approximately 20 μg/ml in a renaturation buffer (0.2M Tris-HCl, pH 9.5, 0.8M arginine, 0.2mM reduced glutathione, IrmM oxidized glutathione). After incubation at 4° C. with stirring for 24 hours, the refolding solution is concentrated and dialyzed against PBS buffer. The refolded protein is further purified by immunoaffinity chromatography using a conformation dependent mAb (e.g., the 2F5 mAb) coupled to GammaBind Plus Sepharose. Aggregates and monomers are removed by Superdex 200 gel filtration column. Similarly, variants starting at different positions after the V3 loop and prior to the start of gp41can be genetically engineered as well, expressed and refolded as potential protein vaccine immunogens.

Example 2.

Crystallization and X-ray Crystallographic Analysis of SIV gp140Trimers

X-ray crystallographic analyses are performed on SIV gp140produced by recombinant mammalian, bacterial, and insect cells (see above). A critical factor for the production of useful crystals is both the chemical and size homogeneity of the macromolecule sample. A major factor contributing to size heterogeneity of glycoproteins is heterogeneous glycosylation. Proteins that are monodisperse under aqueous conditions have a probability of 75% of yielding crystals suitable for x-ray crystallography while polydisperse disperse samples have only a 10% probability of doing so [Sali (1998) Nature Struc. Biol. 5, 1029-1032]. Prior to crystallization, the SIV gp140 sample is analyzed with an instrument (Dyna Pro-ms/x; Protein Solutions, Lakewood, N.J.) designed to obtain a measurement of the degree of size homogeneity of the sample.

The Hampton sparse matrix crystallization screening protocol [Jancarik et al. (1991). J. Appl. Cryst. 24: 409-41 1) is used to ascertain optimal crystallization conditions. The effectiveness of this technique is based on known crystallization conditions for a variety of protein molecules. This sampling technique allows a quick test of wide ranges of pH, buffer type, precipitants, and some commonly used additives for the initial trial. Three categories of precipitants (salts (e.g.ammonium sulfate), PEG (e.g., PEG 4000), and organic solvents are tested. The hanging-droplet vapor diffusion method of crystallization is used such that, for each condition, as little as 1 μl of protein solution (at about 15-20 mg/ml) is used. One-2 mg protein is sufficient for testing 100 different conditions.

The additives used for crystallization can be very important. For example, the detergent β-octyl-glucopyranoside has in some cases been found to be invaluable [e.g., Casasnovas et al. (1997) Nature 387: 312-315]. This detergent shields the hydrophobic surface of the protein. Glycerol is also known to be useful in crystallizing flexible proteins [Sousa et al. (1990) Methods: A Companion to Methods in Enzymology 1, 50-56]. Glycerol was also usefuil in converting twinning crystals into single crystals [Tan (1997) Proc. Nati. Acad. Sci. USA 94:12303-12308]. In addition, Na₂SO₄ dramatically improves the diffraction quality of crystals [Tong (1996) Nature 383: 272-275].

One x-ray crystallographic method of obtaining a novel 3-D structure is the multiple-isomorphous replacement (NMR) method. By examining the amino acid sequence of the protein, a favorable heavy atom-containing compound in which to soak the protein crystals is selected. A number of x-ray crystallographic data sets are collected using soaked and unsoaked crystals. Data sets obtained with an unsoaked crystal are compared to those obtained with soaked crystals to see whether there is any heavy atom binding. This is done by calculating a difference Patterson map. Sometimes a single heavy atom derivative will provide adequate initial phasing as a starting point. If not, other heavy atom-containing compounds are tested. It has been found that xenon is a good anomalous scattering center [Schiltz et al. (1995) Structure 3: 309-316]. The Molecular Structure Corporation (MSC) (Woodlands, Tex.) manufactures a device called Cryo-Xe-Siter™, which allows the introduction of xenon into protein crystals. According to a survey by MSC, the success rate is as high as 50%.

Another technique that has been extremely successful in the protein crystallography field is the MAD (multi-wavelength anomalous dispersion) method [Hendrickson (1991) Science 254, 51-58). About 2-4 data sets are collected from one single frozen crystal on the synchrotron, each using a slightly different wavelength near the absorption edge of the anomalous scattering centers. These data sets are in principle sufficient to obtain phases and solve the structure. To use the MAD method, one can make a seleno-methionine mutant protein and use the selenium as the anomalous scattering center for MAD data collection [Lustbader et al. (1995) Endocrinology 136: 640-650]. The mutant crystal is in general highly isomorphous to the wild type crystal because it avoids non-isomorphorism introduced by heavy atom binding. Although the difference in the number of electrons between sulfur and selenium is only 18, the difference in scattering factor is sufficient to produce prominent peaks in the conventional isomorphous difference Patterson even using the data collected with an in-house x-ray source at the Dana Farber Cancer Institute [Wang (1995) Proc Natl Acad Sci USA 92, 5714-5718]. The selenium-based MAD phasing has become popular for another two reasons. First, the MAD data collection technique using the synchrotron has become routine. Second, there are programs that make it easier to locate the Se sites in crystals. These include SOLVE (Terwilliger et al. (1999) Acta Crystallogr. D Biol. Crystallogr. 55:849-61) and SnB, which is an implementation of the direct method [Hauptman (1999). Acta Crystallogr. A 55:891-900; Weeks (1999) Acta Crystallogr. D Biol. Crystallogr. 55:492-500].

Yet another x-ray crystallographic method is the molecular replacement method. In this method, diffraction data obtained on a new molecule of interest are phased using the 3-D coordinates of another molecule whose 3-D structure is known and can thus be employed as a search model for phasing. A powerful computer program AMoRe [Navaza (1994). Acta Cryst. A50: 157-163] is used to implement the method. A good search model is crucial to yield a correct result with molecular replacement. A problem with the method is that one does not know beforehand exactly how homologous the chosen search model is to the molecule of interest. One way to get around the burden is to take a so-called composite model, i.e., to superimpose several homologous molecules together as a search model. The composite model is then the average structure of several known molecules. Thus, for example, the several known structures of the gp41 ectodomain, or segments thereof, [Weissenhorn et al. (1997) Nature 387:426-430; Chan et al. (1997) Cell 89:263-273; Tan et al. (1998) Proc. Natl. Acad. Sci. USA. 94:12303-12308] could be superimposed to create a search model for the gp41 ectodomain in the gp140 trimer.

Example 3

Designing an immunogenic compound based on the 3-D structure of the ectodomain of gp41 in the SIV gp140 trimer Once the 3-D structure of SIV gp41 in its trimeric, prefusion state is obtained, the information is used to design a candidate immunogen. Given that the 3-D structure of the gp41 region in the gp140 (gp120/gp41) trimer is presently unknown, it is not possible to describe all potential avenues of design. A few examples are presented. One anticipated scenario is that the gp41 fusion peptide and the N-terminal trimeric peptide are buried in the axial groove between the gp120 protomers within the native trimer, leaving only the C-terminal peptide accessible to antibody attack: If this is the case, the C-terminal segment can be produced in E. coli or by peptide synthesis, adopting trimeric or non-trimeric conformation as the case may be. NMR or x-ray crystallography can then be used to show parity of the relevant segment in the mini-protein and the x-ray crystallographically-defined gp140 trimer structures. Alternatively, if this region is exposed but extensively constrained by structural interactions with gp120 or other gp41 components in achieving the native structure, additional domains must be appended. In the latter case, a non-native interaction domain from protein G, immunoglobulin, CD2 or other domains that can be used to facilitate the native fold of the gp41 graft can be generated. Eukaryotic and prokaryotic production is tested in parallel and structural authenticity documented by NMR and/or crystallography. Key parameters for the choice of additional domains to be incorporated into the mini-protein construct are ease of production and the potential to target dendritic cells (i.e., interdigitating dendritic cells) for optimization of immunogenicity. For example, Flt3 ligand, which stimulates growth of dendritic cells and could serve as a targeting vector to bring the mini-protein antigen to dendritic cells, could be co-incorporated with the immunogenic domain.

Example 4.

Testing a Candidate Immunogenic Compound for Immunogenicity

Compounds designed and produced as described in Example 3 are tested in test animals. Animals of choice are rabbits, guinea pigs, or rhesus monkeys. The test animals are injected with and without an adjuvant (see above), by various routes, e.g., parenteral (e.g., intravenous, subcutaneous, or intramuscular), mucosal (e.g., intranasal, intrarectal, or intragastric), and with various frequencies. At various time points, the animals are bled and sera are extracted from the blood. The sera are tested for the presence of antibodies that bind to the test compound, to SIV gp41, to SIV gp140, to SIV gp160, and to intact SIV virions by any of a number of methods known to those in the art. In addition, the sera are tested for the presence of antibodies that neutralize SIV using assays familiar to investigators in the art [see, for example, Cho et al. (2001) J. Virol. 75(5):2224-2234]. Multiple strains of SIV are tested. Cells used for testing are whole peripheral blood mononuclear cells (PBMC), T cell lines (e.g., the CEMx174 cell line), or macrophage cell lines. PBMC can be activated (e.g., by a lectin such concanavalin A or phytohemagglutin) or resting.

Thus, for example, neutralization assays are performed on the molecularly cloned SIV stocks SIVmac239 and SIVsmH-4, and on the uncloned stocks SIV/DeltaB670 and SIVmac251 (mac32H (pJ5) equivalent). Virus stocks are prepared in H9 cells except for SIVmac239, which was produced in human PBMC. The SIVmac251 stock is extensively passaged in T cell lines. Cell free virus (50 μl containing 0.5 to 1 ng of SIV p27) is added to multiple dilutions of the test sera in 100 μl of growth medium in triplicate wells of 96-well tissue culture plates, which are incubated at 37° C. for 30 minutes before addition of CEMx174 cells (10⁵ cells in 100 μl per well). Cell densities are reduced several-fold and medium is replaced after 3 days of incubation. The incubation is continued until virus-induced syncytium formation and cell killing are observed microscopically in wells incubated in the absence of test sera. Neutralization is determined by staining viable cells with Finters's neutral red in poly-L-lysine coated plates and measuring the A₅₄₀ of each well. Neutral red uptake by CEMx174 cells is linear from 3.1×10⁴ to 5×10⁵ viable cells/well, corresponding to A₅₄₀ values of 0.25 to 1.6. Percent protection is calculated by the difference in A₅₄₀ between test wells (wells containing cells plus virus plus test sera) and virus control wells (wells containing cells plus virus), divided by the difference in A₅₄₀ between cell control wells (wells containing cells only) and virus control wells. Data are expressed as ID₅₀, which is the dilution of serum necessary to protect cells from virus-induced death to a level of 50%.

In addition to in vitro neutralization assays, in vilpo protection assays such as those described generally above can be performed.

A compound demonstrating immunogenicity by any of the above assays can be manufactured by any of the methods described herein.

While the above examples describe experiments dealing with an SIV analysis, those of skill in the art will appreciate that the analysis can be readily adapted to the production of an HIV- (e.g., HIV-1- or HIV-2-) specific immunogenic compound.

Example 5.

Generation of an HIV-1 Immunogen

A genetic construct encoding a fusion protein including an HV-1 gp41 ectodomain was generated by PCR and cloned into the T7 promoter-containing expression vector pET11a. The genetic construct contained cDNA encoding, 5′ to 3′, domains consisting of: (a) 58 amino acids of the B1 IgG binding domain of streptococcal protein G (“GB 1”); (b) 57 amino acids of the C terminal ectodomain (cte) of HIV-1 strain HIV-1ada (clade B) gp41; and (c) a 31 amino acid, mutated segment of the Saccharomyces cerevisiae leucine zipper protein GCN4. The amino acid sequence (SEQ ID NO:15) of the fusion protein, designated GCG2, is shown in FIG. 4A; the first amino acid in each domain is indicated in italics.

The 57 amino acid HIV-1 cte domain (SEQ ID NO:16) (FIG. 4B) included an amino acid sequence (SEQ ID NO:17) (FIG. 4C) corresponding to the C-domain sequence (having the amino acid sequence SEQ ID NO:14 shown in the “ALL” chart in FIG. 1) that, on account its low polymorphism and its predicted location on the surface of gp41 in its trimeric, preflusion state (see above), is considered a promising candidate for immunogen development. The GB1 domain was included in GCG2 to facilitate purification and to enhance the immunogenicity and solubility of the protein. The GCN4 domain was included in GCG2 to enhance trimerization of the protein so as to mimic the conformation of the cte fragment as it would occur in a native. gp120/gp41 complex.

GCG2 was produced in BL21 (DE3) E coli bacteria essentially as described above for SIV gp140and was purified by IgG affinity, ion exchange, and gel filtration chromatography. One hundred mg of soluble GCG2 was produced from 1 liter of bacteria.

As shown by immunoprecipitation, the broadly neutralizing anti-mAbs 2F5 and 4E10 both bound GCG2 (FIG. 5). In addition, the ability of two mAbs (98.6 and 126.6) that recognize immunodominant cluster II of gp41 to bind to GCG2 were tested by Biosensor analysis. mAb 98.6 (or mAb 126.6) was bound to a CM5 chip which was then exposed to purified GB1 domain to prevent non-specific binding of GCG2 to the Fc domain of the chip-bound mAb. GCG2 was incubated with purified Fc fragments (also to prevent non-specific binding of GCG2 to the Fc domain of the mAb on the chip) and then passed over the chip in the Biosensor to measure binding to the chip-bound mAb. A control Biosensor response obtained when GCG2 was analyzed in the same way but with a control mAb of irrelevant specificity bound to the chip was subtracted from the responses observed with the 98.6 and 126.6 mAbs. While GCG2 bound to mAb 98.6, no significant binding was detected with mAb 126.6 (FIG. 6). Since mAb 98.6 recognizes immunodominant cluster II in both pre-hairpin and hairpin conformations of gp41 and mAb recognizes immunodominant cluster II in only the hairpin conformation of gp41, the above data indicate that, in GCG2, the HIV cte domain is in the pre-hairpin conformation. gp41 in an HIV-1 virion assumes the pre-hairpin conformation subsequent to binding of a relevant gp120/gp41 complex to CD4 and a coreceptor on a potential host cell (e.g., a T cell or a macrophage). By assuming this pre-hairpin conformation, gp41 becomes capable of inserting its amino-terminal fusion-peptide domain into the cell membrane of the potential host cell. Insertion of gp41 into the cell membrane facilitates fusion with the cell membrane and hence infection of the host cell by the virion. It seems likely thus that GCG2 would be an immunogen capable of eliciting the production (in appropriate mammalian subjects) of antibodies that bind to gp41 in its pre-hairpin conformation. By binding in such a highly selective manner to gp41 as it exists in virions at the stage immediately prior to fusion of HIV-1 with a host cell membrane, these antibodies would likely be potent inhibitors of infection of cells by mV-1.

A number of embodiments of the invention have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, the invention is limited only by the following claims. 

1. A computer-assisted method of generating an immunogen, the method requiring use of a programmed computer comprising a processor and an input device, the method comprising: (a) providing a pathogenesis factor (PF), or a fragment of a PF, comprising a region with low polymorphism, wherein the region is in an active conformation; (b) obtaining data on the region in the active conformation, wherein the data can be used to determine the three-dimensional structure of the region in the active conformation; (c) inputting to the input device the data; (d) determining, using the processor, the three-dimensional structure of the region in the active conformation; (e) designing a compound comprising a domain that includes at least one epitope with the ability to induce the production in a mammal of an antibody that binds to the region in the active conformation, (f) producing the compound; and (g) determining whether the compound is an immunogen in a mammalian host.
 2. A process of manufacturing a compound, the process comprising: carrying out the method of claim 1; and, after determining that the compound is an immunogen, manufacturing the compound.
 3. A method of testing a compound for prophylactic activity, the method comprising administering a compound made by the method of claim 2 to a mammal and testing for the presence in the mammal of antibodies that inhibit the pathogenicity of a pathogenic agent of which the PF is (a) a component or (b) an altered form of a component, wherein the presence in the mammal of antibodies that inhibit the pathogenicity of the pathogenic agent is an indication that the compound has prophylactic activity against the pathogenic agent.
 4. The method of claim 1, wherein the PF is a component, or an altered form of a component, of an infectious microorganism.
 5. The method of claim 4, wherein the infectious microorganism is a microorganism that replicates inside a cell.
 6. The method of claim 5, wherein the microorganism is a virus.
 7. The method of claim 6, wherein the virus is a retrovirus.
 8. The method of claim 7, wherein the retrovirus is simian immunodeficiency virus (SIV) or human immunodeficiency virus (HIV).
 9. The method of claim 5, wherein the microorganism is a protozoan parasite.
 10. The method of claim 9, wherein the protozoan parasite is a malarial protozoan parasite.
 11. The method of claim 10, wherein the PF is merozoite surface protein-1 (MSP-1) or ring-infected erythrocyte surface antigen (RESA).
 12. The method of claim 10, wherein the PF is selected-from the group consisting of Plasmodium falciparum erythrocyte membrane protein-1(PfEMP-1), Plasmodium falciparum 332 antigen (Pf332), Rosettin, merozoite surface protein-2 (MSP-2), serine stretch protein (SERP), glutamate-rich protein (GLURP), apical membrane antigen-1 (AMA-1), and histidine-rich protein-2 (HRP-2).
 13. The method of claim 1, wherein the PF is: (a) a naturally occurring polypeptide; (b) an altered form of a naturally occurring polypeptide; or (c) a molecular complex comprising two or more subunits, each subunit being either of (a) or (b).
 14. The method of claim 13, wherein the PF comprises a complex of retroviral envelope glycoproteins.
 15. The method of claim 14, wherein the PF comprises three recombinant SIV gp140 polypeptides.
 16. The method of claim 1, wherein the PF is a component, or an altered form of a component, of a cancer cell.
 17. The method of claim 16, wherein the PF is prostate-specific membrane antigen (PSMA).
 18. The method of claim 4, wherein the microorganism is a bacterium.
 19. The method of claim 5, wherein the PF, or a wild-type form of the PF, mediates entry of the microorganism into a cell.
 20. The method of claim 19, wherein the cell is a CD4+ cell.
 21. The method of claim 20, wherein the CD4+ cell is a T cell.
 22. The method of claim 20, wherein the CD4+ cell is a monocyte or a macrophage.
 23. The method of claim 19, wherein the cell is an erythrocyte.
 24. The method of claim 1, wherein the PF is provided in a crystalline form and the data are a criteria data set comprising three-dimensional atomic coordinates.
 25. A compound made by the process of claim
 2. 26. A method of inducing an immune response in a mammal, the method comprising administering the compound of claim 25 to the mammal.
 27. The method of claim 26, wherein the immune response is a protective immune response.
 28. The method of claim 26, wherein the compound is administered parenterally to the mammal.
 29. The method of claim 26, wherein the compound is administered intranasally or transcutaneously. 